EU Representation
Representing non-EU based manufacturers in a successful EU Market entry and safeguarding their future across the entire community.
Learn MoreEU Product Registration
Ensuring compliance and registering products to be made available on the EU Market.
Learn MoreTechnical Documentation Review & EU Submissions
For your products to legally enter the EU Market and continue to circulate, you must have valid documentation.
Learn MoreEU Consultancy, Legal & Training
Find your way through a complicated EU marketplace with the support of a professional.
Learn MoreCareers at Obelis
Take the first step to a consulting career that helps build a safer Europe.
Learn MoreTestimonials
We have provided compliance and consulting services for more than 3000 manufacturers in over 60 countries, helping them successfully introduce products to the European market.
Learn MoreContact Us
Our head office is in Brussels and we have a network of offices in 11 different countries including the US and Israel.
Learn MoreInternational Representatives
An experienced EU compliance representative is just a call or meeting away…
Learn MoreObelis International Offices (OIO) Network
Obelis International Offices are independent partners who are able to provide our clients with solutions in other global markets of their choosing.
Learn MoreWebinar: Complying with the MDR

The new Medical Device Regulation will be fully applicable as of May 26, 2021, therefore you need to make sure you know how to manage your Legacy Devices Compliance on the EU Market.
In this webinar, we will provide an overview of:
- How to register as actor to EUDAMED: step-by-step explanation
- Your Legacy Device documentation review: requirements & services